Transcript Prezentace aplikace PowerPoint

Conversion of amino acids to
specialized products
a-nitrogen atom of amino acids is a
primary source for many nitrogenous
compounds:
Heme
Purines and pyrimidines
Hormones
Neurotransmitters
Biologically active peptides
Glycine
Glycine is used for heme, purine, creatin, and
glutathione synthesis
a-carbon and a-nitrogen atoms of glycine are used
for synthesis of porphyrine, prosthetic group of
heme.
Take over: http://www.rpi.edu/dept/bcbp/molbiochem/MBWeb/mb2/part1/heme.htm
Synthesis of heme
1. Condensation of 1 glycine and 1 succinylCoA by the pyridoxal
phosphate-containing enzyme, d-aminolevulinic acid
synthase (ALA synthase) in mitochondria.
Take over: http://www.rpi.edu/dept/bcbp/molbiochem/MBWeb/mb2/part1/heme.htm
2. d-aminolevulinic acid (ALA)  cytosol.
3. Dimerization of 2 molecules of ALA to produce the
pyrrole ring - compound porphobilinogen – precursor
for porphyrine synthesis (porfobilinogen synthase or
ALA dehydratase)
Take over: http://www.rpi.edu/dept/bcbp/molbiochem/MBWeb/mb2/part1/heme.htm
Glycine is incorporated intact as
constituent of purines.
Synthesis of creatine and creatinine
• Creatine (methyl guanidino
acetic acid) – nitrogenous organic
acid - helps to supply energy to
muscle.
• Creatine  conversion to
creatine phosphate - a storage
form of high energy phosphate in
vertebrate muscles.
•
• The amount of creatinine
produced is related to muscle
mass.
• The level of creatinine excretion
(clearance rate) is a measure of
renal function.
Take over http://www.indstate.edu/thcme/mwking/aminoacidderivatives.html
Synthesis of glutathione (GSH)
The role of GSH as a reductant is extremely
important - erythrocytes.
Reduced form – GSH, oxidized form GSSG.
In the reduced state, the thiol group of cysteine
is able to donate a reducing equivalent (H++
e−) to other unstable molecul
Endogenously produced H2O2 during oxygen
transport is reduced by GSH in the presence
of selenium-dependent GSH peroxidase.
The enzyme glutathione reductase utilizes
NADPH as a cofactor.
It is used in metabolic and biochemical reactions
- DNA synthesis and repair, protein
synthesis, prostaglandin synthesis, amino
acid transport, and enzyme activation.
The role of GSH in detoxification of xenobiotics
 formation of conjugates with GSH
(spontaneously or enzymatically) 
excretion from the cell, in the case of liver –
to the bile.
Take over: http://www.rpi.edu/dept/bcbp/molbiochem/MBWeb/mb1/MB1index.html
The biologically active amines formed
by decarboxylation of amino acids
Catecholamines
(dopamine norepinephrine, epnephrine)
g-aminobutyric acid (GABA)
Serotonine, melatonine
Histamine
Polyamines
Tyrosine-Derived Neurotransmitters
•
A catecholamine (CA) - monoamine compound, has a catechol (benzene
with two -OH side groups) and a side-chain amine.
•
dopamine, norepinephrine, and epinephrine.
•
Adaptation to variety of acute and chronic stress.
•
Dietary tyrosine – transport to the sites of synthesis (brain catecholamine-secreting neurons and the adrenal medulla).
•
Norepinephrine (NE) and epinephrine (E) acts via specific adrenergic
receptors – a1, a2 and b coupled with G proteins, dopamine binds to
dopamineric receptors.
•
The action of E and NE in the liver, the adipocyte, the skeletal miscle
directly influence fuel metabolism (glycogenolysis, lipolysis).
Synthesis of the catecholamines from tyrosine
1.
2.
3.
4.
5.
Tyrosine hydroxylase
requires
tetrahydrobiopterin as
cofactor.
The hydroxylation
reaction generates
DOPA. (3,4dihydrophenylalanine)
DOPA decarboxylase
converts DOPA to
dopamine.
Dopamine bhydroxylase converts
dopamine to
norepinephrine.
Phenylethanolamine Nmethyltransferase
converts norepinephrine
to epinephrine.
Take over: http://themedicalbiochemistrypage.org/amino-acid-metabolism.html
Degradation of catecholamines
Oxidative deamination by monoamine oxidase (MAO)
Oxidation and methylation by
catecholamine-O-methyl transferase
(COMT) convert the products to
metanephrines and vanillmandelic acid
(4-hydroxy-3-methoxymandelic acid).
Degradation of catecholamines
Treatment of Parkinson's disease
g-amino butyric acid (GABA)
• Major inhibitory neurotransmitter in the CNS.
•GABAergic function plays a role
in many neurological and
psychiatric disorders (its lack
leads to convulsions, epilepsia).
• Directly regulates muscle
tone.
• Involved in mechanism of
memory.
Tryptophan
Tryptopan serves as the precursor for the
synthesis of serotonin and melatonin
1.
2.
3.
4.
Hydroxylation reaction (tryptophan-5monooxygenase)
Decarboxylation (aromatic L-amino
acid decarboxylase)
Acetylation (serotonin N-acetylase)
Conversion to melatonin
(hydroxyindole-O-methyltransferase).
Take of textbook: D. L. Nelson, M. M. Cox: Lehninger Principle of Biochemistry. Fourt Deition.
Serotonin and melatonin
• Serotonin - 90% of serotonin is found in the digestive
tract and in blood platelets (powerfull vasoconstrictor, in the
gastrointestinal tract (mediates gut movements).
• Lesser amounts are found in the brain and the retina
(cannot cross the blood-brain barrier)
• The role of serotonin in CNS – synthesis in serotonergic
neurons, regulation of mood, appetite, sleep, cognitive
functions (memory and learning).
• Imbalance in serotonin levels may influence mood in a
way that leads to depression (antidepressants inhibit
reuptake process of serotonin)
Serotonin and melatonin
• Melatonin regulates circadian rhythms, acts as a
synchronizer of the biological clock
• Synthesis and secretion of melatonin increases during the
dark period of the day.
• Concentration maintained at a low level during daylight
hours.
• Melatonin is a powerful free-radical scavenger - direct
scavenger of radical oxygen and nitrogen species including OH, O2−, and NO .
Histidine
• Carnosine is the dipeptide of the
amino acids b-alanine and histidine.
• Carnosine is highly concentrated in
muscle and brain tissues.
• Scavenger of ROS (radical oxygen
species).
•
Protects cells against lipoperoxidation
• Membrane fatty acids during oxidative
stress.
• Possibly improving Alzheimer´s
disease through inhibition of growing an
aggregates of b-amiloid proteins in the
brain.
Carnosine
Histamine
•
•
Histamine is derived from the
decarboxylation of the amino acid
histidine.
Biogenic amine regulating physiological
function in the gut and acting as a
neurotransmitter - regulates
physiological function in the gut and
acts as a neurotransmitter Histamine
triggers the inflammatory response.
Causes several allergic symptoms.
1. It contributes to an inflammatory
response.
2. It causes constriction of smooth muscle.
3. Is cause second type of allergic
response (one of the major causes for
asthma)
Polyamines
•
Polyamines are highly cationic and
tend to bind nucleic acids with high
affinity.
•
Regulation of DNA, RNA synthesis,
protein synthesis diring
embryogenesis.
•
Important modulators of a variety
of ion channels (potassium channel).
•
Growth factors in both eucaryotic
and procaryotic cells.
Take over: http://themedicalbiochemistrypage.org/amino-acid-metabolism.html
Nitric Oxide NO
• Nitric oxide (NO) is produced by vascular
endothelium and smooth muscle, cardiac
muscle, and many other cell types.
• The substrate for NO is L-arginine that is
transported into the cell.
•Nitric oxide serves many important
functions:
•Vasodilation (ligand mediated and flow
dependent)
•Inhibition of vasoconstrictor influences (e.g.,
inhibits angiotensin II and sympathetic
vasoconstriction)
•Inhibition of platelet adhesion to the vascular
endothelium (anti-thrombotic)
•Inhibition of leukocyte adhesion to vascular
endothelium (anti-inflammatory)
•Antiproliferative action (e.g., inhibits smooth
muscle hyperplasia following vascular injury)
•Scavenging superoxide anion (antiinflammatory)